FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
FLOSWITCH(R) HP
K Number: K913871
·
Decision Nov 25, 1991
Classifications
1
FEI Numbers
213
Registration Numbers
214
Same Product Code
497
Applicant Total
430
Review Days
89
Basic Information
- Device Name
- FLOSWITCH(R) HP
- K Number
- K913871
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1200
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- BOSTON SCIENTIFIC CORP.
- Date Received
- August 28, 1991
- Decision Date
- November 25, 1991
- Product Code
- DQO
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| DQO | Catheter, Intravascular, Diagnostic | FDA class 2 | Cardiovascular |
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